2. Gene
  3. FOXH1 - forkhead box H1 Gene

FOXH1 - forkhead box H1 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as FAST1; FAST-1

Gene ID: 8928 | Gene type: protein coding

About FOXH1

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:144,473,412-144,475,849 (from NCBI)

This gene has 2 transcripts (splice variants), 192 orthologues, 42 paralogues and is associated with 6 phenotypes. Broad expression in skin (RPKM 10.3), brain (RPKM 5.3) and 22 other tissues.

Summary

FOXH1 encodes a human homolog of Xenopus forkhead activin signal transducer-1. FOXH1 protein binds SMAD2 and activates an activin response element via binding the DNA motif TGT(G/T)(T/G)ATT. [provided by RefSeq, Jul 2008]

FOXH1 Products(1)

mRNA Protein Name
NM_003923.3 NP_003914.1 forkhead box protein H1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
contributes to DNA binding IDA
IDA: Inferred from direct assay
9389648 GOA
contributes to DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
17438144 GOA
enables DNA-binding transcription factor binding IPI
IPI: Inferred from physical interaction
18922797 GOA
enables R-SMAD binding IMP
IMP: Inferred from mutant phenotype
16120611 GOA
enables R-SMAD binding IPI
IPI: Inferred from physical interaction
9389648 GOA
enables SMAD binding IPI
IPI: Inferred from physical interaction
21828274 GOA
enables bHLH transcription factor binding IPI
IPI: Inferred from physical interaction
21828274 GOA
enables co-SMAD binding IMP
IMP: Inferred from mutant phenotype
16120611 GOA
enables nuclear androgen receptor binding IPI
IPI: Inferred from physical interaction
16120611 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9702198 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
9702198 GOA
enables sequence-specific DNA binding IDA
IDA: Inferred from direct assay
9702198 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cellular response to cytokine stimulus IMP
IMP: Inferred from mutant phenotype
14671321 GOA
involved in negative regulation of DNA-binding transcription factor activity IDA
IDA: Inferred from direct assay
16120611 GOA
involved in negative regulation of androgen receptor signaling pathway IDA
IDA: Inferred from direct assay
16120611 GOA
involved in negative regulation of intracellular estrogen receptor signaling pathway IDA
IDA: Inferred from direct assay
16120611 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
9389648 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
9702198 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
14671321 GOA
Cellular Component GO Annotation Evidence Reference Source
part of activin responsive factor complex IDA
IDA: Inferred from direct assay
9389648 GOA
located in chromatin IDA
IDA: Inferred from direct assay
21828274 GOA
located in nucleus IDA
IDA: Inferred from direct assay
16120611 GOA
part of transcription regulator complex IDA
IDA: Inferred from direct assay
17438144 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

FOXH1 Protein Structure

Forkhead

Forkhead: Forkhead domain (33 - 114)

  • 0
  • 100
  • 200
  • 300
  • 365 a.a.
Protein Preferred Names Protein Names

forkhead box protein H1

TGF-beta/activin signal transducer

FOXH1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra FOXH1 O75593 PNMA5 Homo sapiens Q96PV4
Validated Y2H
32296183
Intra FOXH1 O75593 TEKT5 Homo sapiens Q96M29
Validated Y2H
32296183
Intra FOXH1 O75593 TEKT5 Homo sapiens Q96M29
Y2H Array
32296183
Intra FOXH1 O75593 TEKT5 Homo sapiens Q96M29
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP13-3 Homo sapiens Q3SY46
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP13-3 Homo sapiens Q3SY46
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP13-3 Homo sapiens Q3SY46
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP19-7 Homo sapiens Q3SYF9
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP19-7 Homo sapiens Q3SYF9
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP19-7 Homo sapiens Q3SYF9
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 SMAD2 Homo sapiens Q15796
Y2H Array
32296183
Intra FOXH1 O75593 SMAD2 Homo sapiens Q15796
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 SMAD2 Homo sapiens Q15796
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP11-1 Homo sapiens Q8IUC1
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP11-1 Homo sapiens Q8IUC1
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP11-1 Homo sapiens Q8IUC1
Y2H Array
32296183
Intra FOXH1 O75593 ZIC1 Homo sapiens Q15915
Validated Y2H
32296183
Intra FOXH1 O75593 ACTMAP Homo sapiens Q5BKX5-3
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 ACTMAP Homo sapiens Q5BKX5-3
Y2H Array
32296183
Intra FOXH1 O75593 ACTMAP Homo sapiens Q5BKX5-3
Validated Y2H
32296183
Intra FOXH1 O75593 RBPMS2 Homo sapiens Q6ZRY4
Validated Y2H
32296183
Intra FOXH1 O75593 RBPMS2 Homo sapiens Q6ZRY4
Y2H Array
32296183
Intra FOXH1 O75593 RBPMS2 Homo sapiens Q6ZRY4
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HSF4 Homo sapiens Q9ULV5-2
Validated Y2H
32296183
Intra FOXH1 O75593 HSF4 Homo sapiens Q9ULV5-2
Y2H Array
32296183
Intra FOXH1 O75593 HSF4 Homo sapiens Q9ULV5-2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 UFSP1 Homo sapiens Q6NVU6
Validated Y2H
32296183
Intra FOXH1 O75593 UFSP1 Homo sapiens Q6NVU6
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 UFSP1 Homo sapiens Q6NVU6
Y2H Array
32296183
Intra FOXH1 O75593 RBM46 Homo sapiens Q8TBY0
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 RBM46 Homo sapiens Q8TBY0
Y2H Array
32296183
Intra FOXH1 O75593 RBM46 Homo sapiens Q8TBY0
Validated Y2H
32296183
Intra FOXH1 O75593 FAM168B Homo sapiens A1KXE4-2
Y2H Array
32296183
Intra FOXH1 O75593 FAM168B Homo sapiens A1KXE4-2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP19-2 Homo sapiens Q3LHN2
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP19-2 Homo sapiens Q3LHN2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP19-2 Homo sapiens Q3LHN2
Validated Y2H
32296183
Intra FOXH1 O75593 PRR20D Homo sapiens P86480
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 PRR20D Homo sapiens P86480
Validated Y2H
32296183
Intra FOXH1 O75593 PRR20D Homo sapiens P86480
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP19-6 Homo sapiens Q3LI70
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP19-6 Homo sapiens Q3LI70
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP19-6 Homo sapiens Q3LI70
Y2H Array
32296183
Intra FOXH1 O75593 TSC1 Homo sapiens Q86WV8
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 TSC1 Homo sapiens Q86WV8
Validated Y2H
32296183
Intra FOXH1 O75593 TSC1 Homo sapiens Q86WV8
Y2H Array
32296183
Intra FOXH1 O75593 C10orf55 Homo sapiens Q5SWW7
Validated Y2H
32296183
Intra FOXH1 O75593 C10orf55 Homo sapiens Q5SWW7
Y2H Array
32296183
Intra FOXH1 O75593 C10orf55 Homo sapiens Q5SWW7
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 ATP23 Homo sapiens Q9Y6H3
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 ATP23 Homo sapiens Q9Y6H3
Validated Y2H
32296183
Intra FOXH1 O75593 ATP23 Homo sapiens Q9Y6H3
Y2H Array
32296183
Intra FOXH1 O75593 OXER1 Homo sapiens Q8TDS5
Y2H Array
32296183
Intra FOXH1 O75593 OXER1 Homo sapiens Q8TDS5
Validated Y2H
32296183
Intra FOXH1 O75593 OXER1 Homo sapiens Q8TDS5
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 AOC1 Homo sapiens P19801
Validated Y2H
32296183
Intra FOXH1 O75593 AOC1 Homo sapiens P19801
Y2H Array
32296183
Intra FOXH1 O75593 AOC1 Homo sapiens P19801
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 FAM83A Homo sapiens Q86UY5
Y2H Array
32296183
Intra FOXH1 O75593 FAM83A Homo sapiens Q86UY5
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 FAM83A Homo sapiens Q86UY5
Validated Y2H
32296183
Intra FOXH1 O75593 NOTO Homo sapiens A8MTQ0
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 NOTO Homo sapiens A8MTQ0
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP7-1 Homo sapiens Q8IUC3
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP7-1 Homo sapiens Q8IUC3
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP7-1 Homo sapiens Q8IUC3
Y2H Array
32296183
Intra FOXH1 O75593 UBAP2 Homo sapiens Q5T6F2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 UBAP2 Homo sapiens Q5T6F2
Y2H Array
32296183
Intra FOXH1 O75593 UBAP2 Homo sapiens Q5T6F2
Validated Y2H
32296183
Intra FOXH1 O75593 SMAD3 Homo sapiens P84022
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 SMAD3 Homo sapiens P84022
Y2H Array
32296183
Intra FOXH1 O75593 SMAD3 Homo sapiens P84022
Validated Y2H
32296183
Intra FOXH1 O75593 TFG Homo sapiens Q92734
Validated Y2H
32296183
Intra FOXH1 O75593 CYSRT1 Homo sapiens A8MQ03
Y2H Array
32296183
Intra FOXH1 O75593 CYSRT1 Homo sapiens A8MQ03
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 NCK1 Homo sapiens P16333
Peptide Array
17474147
Intra FOXH1 O75593 TLX3 Homo sapiens O43711
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 TLX3 Homo sapiens O43711
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP3-3 Homo sapiens Q9BYR6
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP3-3 Homo sapiens Q9BYR6
Y2H Array
32296183
Intra FOXH1 O75593 KRTAP3-3 Homo sapiens Q9BYR6
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 CEACAM6 Homo sapiens P40199
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 CEACAM6 Homo sapiens P40199
Validated Y2H
32296183
Intra FOXH1 O75593 CEACAM6 Homo sapiens P40199
Y2H Array
32296183
Intra FOXH1 O75593 SERGEF Homo sapiens Q9UGK8
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 SERGEF Homo sapiens Q9UGK8
Validated Y2H
32296183
Intra FOXH1 O75593 SERGEF Homo sapiens Q9UGK8
Y2H Array
32296183
Intra FOXH1 O75593 PPP1R37 Homo sapiens O75864
Validated Y2H
32296183
Intra FOXH1 O75593 AR Homo sapiens P10275
Anti Bait CoIP
16120611
Intra FOXH1 O75593 MSX2 Homo sapiens P35548
Validated Y2H
32296183
Intra FOXH1 O75593 MSX2 Homo sapiens P35548
Y2H Array
32296183
Intra FOXH1 O75593 MSX2 Homo sapiens P35548
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HLX Homo sapiens Q14774
Validated Y2H
32296183
Intra FOXH1 O75593 HLX Homo sapiens Q14774
Y2H Array
32296183
Intra FOXH1 O75593 HLX Homo sapiens Q14774
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 CRYBA1 Homo sapiens P05813
Validated Y2H
32296183
Intra FOXH1 O75593 CRYBA1 Homo sapiens P05813
Y2H Array
32296183
Intra FOXH1 O75593 CRYBA1 Homo sapiens P05813
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 MAGED1 Homo sapiens Q9Y5V3
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 MAGED1 Homo sapiens Q9Y5V3
Validated Y2H
32296183
Intra FOXH1 O75593 CFAP68 Homo sapiens Q9H5F2
Validated Y2H
32296183
Intra FOXH1 O75593 CFAP68 Homo sapiens Q9H5F2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 CFAP68 Homo sapiens Q9H5F2
Y2H Array
32296183
Intra FOXH1 O75593 TCF12 Homo sapiens Q99081
Anti Bait CoIP
21828274
Intra FOXH1 O75593 HEY1 Homo sapiens Q9Y5J3
Y2H Array
32296183
Intra FOXH1 O75593 HEY1 Homo sapiens Q9Y5J3
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HEY1 Homo sapiens Q9Y5J3
Validated Y2H
32296183
Intra FOXH1 O75593 DAZAP2 Homo sapiens Q15038
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 DAZAP2 Homo sapiens Q15038
Validated Y2H
32296183
Intra FOXH1 O75593 DAZAP2 Homo sapiens Q15038
Y2H Array
32296183
Intra FOXH1 O75593 KLHL26 Homo sapiens Q53HC5
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KLHL26 Homo sapiens Q53HC5
Validated Y2H
32296183
Intra FOXH1 O75593 PLA2G10 Homo sapiens O15496
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 PLA2G10 Homo sapiens O15496
Y2H Array
32296183
Intra FOXH1 O75593 HOXA1 Homo sapiens P49639
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HOXA1 Homo sapiens P49639
Validated Y2H
32296183
Intra FOXH1 O75593 HOXA1 Homo sapiens P49639
Y2H Array
32296183
Intra FOXH1 O75593 ZC3H10 Homo sapiens Q96K80
Validated Y2H
32296183
Intra FOXH1 O75593 BATF2 Homo sapiens Q8N1L9
Validated Y2H
32296183
Intra FOXH1 O75593 BATF2 Homo sapiens Q8N1L9
Y2H Array
32296183
Intra FOXH1 O75593 BATF2 Homo sapiens Q8N1L9
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HDHD3 Homo sapiens Q9BSH5
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 HDHD3 Homo sapiens Q9BSH5
Validated Y2H
32296183
Intra FOXH1 O75593 HDHD3 Homo sapiens Q9BSH5
Y2H Array
32296183
Intra FOXH1 O75593 CRX Homo sapiens O43186
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 CRX Homo sapiens O43186
Y2H Array
32296183
Intra FOXH1 O75593 TCF3 Homo sapiens P15923
Anti Bait CoIP
21828274
Intra FOXH1 O75593 ATXN1L Homo sapiens P0C7T5
Validated Y2H
32296183
Intra FOXH1 O75593 ATXN1L Homo sapiens P0C7T5
Y2H Array
32296183
Intra FOXH1 O75593 ATXN1L Homo sapiens P0C7T5
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 ZNF503 Homo sapiens Q96F45
Y2H Array
32296183
Intra FOXH1 O75593 ZNF503 Homo sapiens Q96F45
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 ZNF503 Homo sapiens Q96F45
Validated Y2H
32296183
Intra FOXH1 O75593 SOX14 Homo sapiens O95416
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 SOX14 Homo sapiens O95416
Y2H Array
32296183
Intra FOXH1 O75593 SOX14 Homo sapiens O95416
Validated Y2H
32296183
Intra FOXH1 O75593 LASP1 Homo sapiens Q14847-2
Validated Y2H
32296183
Intra FOXH1 O75593 LASP1 Homo sapiens Q14847-2
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 LASP1 Homo sapiens Q14847-2
Y2H Array
32296183
Intra FOXH1 O75593 ARID5A Homo sapiens Q03989
Complementation
32296183
Intra FOXH1 O75593 ARID5A Homo sapiens Q03989
Validated Y2H
32296183
Intra FOXH1 O75593 ARID5A Homo sapiens Q03989
Y2H Array
32296183
Intra FOXH1 O75593 ARID5A Homo sapiens Q03989
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP3-1 Homo sapiens Q9BYR8
Y2H Prey Pooling
32296183
Intra FOXH1 O75593 KRTAP3-1 Homo sapiens Q9BYR8
Validated Y2H
32296183
Intra FOXH1 O75593 KRTAP3-1 Homo sapiens Q9BYR8
Y2H Array
32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Septopreoptic Holoprosencephaly

Septopreoptic Hpe
Midline Interhemispheric Variant Of Holoprosencephaly

Mih

Mih Type Hpe

Mihf

Mihv

Middle Interhemispheric Fusion Variant

Middle Interhemispheric Variant Of Holoprosencephaly

Syntelencephaly
Microform Holoprosencephaly

Hpe, Minor Form

Hpe-L

Holoprosencephaly, Minor Form

Holoprosencephaly-Like

Microform Hpe
Lobar Holoprosencephaly
Alobar Holoprosencephaly
Semilobar Holoprosencephaly
Holoprosencephaly

Holoprosencephaly Sequence

Hpe

Hpe - [Holoprosencephaly]
Acquired Hyperkeratosis

Acquired Keratoderma

Keratoderma - Acquired

Keratoderma, Acquired

Keratosis Blennorrhagica
Friedreich Ataxia

Friedreich Ataxia 1

FRDA

Friedreich Ataxia With Retained Reflexes

Frda1

Fa

Friedreich'S Ataxia

Hereditary Spinal Ataxia

Fa1

Friedreich'S Tabes

Hereditary Spinal Sclerosis

Spinocerebellar Ataxia, Friedreich

Friedreich Spinocerebellar Ataxia

Friedrich'S Ataxia
Holoprosencephaly 4

HPE4

Holoprosencephaly-4

Holoprosencephaly, Type 4
Transposition Of The Great Arteries, Dextro-Looped

Transposition Of The Great Arteries

DTGA1

Dextro-Looped Transposition Of The Great Arteries

DTGA

Congenitally Uncorrected Transposition Of The Great Arteries

Congenitally Uncorrected Transposition Of The Great Vessels

D-Tga

Isolated Ventriculoarterial Discordance

Ventriculoarterial Discordance With Atrioventricular Concordance

Dextro-Transposition Of The Great Arteries

Transposition Of The Great Vessels

Great Vessels Transposition

Transposition Of The Great Arteries, Dextro-Looped 1

Arteries, Great, Transposition, Dextro-Looped

Ventriculoarterial Discordance, Isolated

D-Transposition Of The Great Arteries

Complete Transposition

Tga

Tgv

Transposition Of Great Vessels

Transposition Of The Great Arteries Dextro-Looped 1

Dextro-Looped Transposition Of The Great Arteries 1

Discordant Ventriculoarterial Connection

Complete Transposition Of Great Vessels

Great Vessels Complete Transposition

Total Great Vessel Transposition

Transposition Of Great Arteries

Complete Tga - [Transposition Of The Great Arteries]

Tga - [Transposition Of Great Arteries]

Tgv - [Transposition Of Great Vessels]

Transposition Of Great Vessels Nos

Transposed Vessels Nos
Hypoplastic Right Heart Syndrome

Right Hypoplastic Heart Syndrome
Cardiomyopathy, Familial Hypertrophic, 3

Hypertrophic Cardiomyopathy 3

CMH3

Cardiomyopathy, Hypertrophic, 3

Cardiomyopathy Familial Hypertrophic 3

Cardiomyopathy, Familial Hypertrophic 3

Cardiomyopathy, Hypertrophic, Familial, Type 3
Holoprosencephaly 3

HPE3

Hlp3

Holoprosencephaly-3

Holoprosencephaly, Type 3
Patau Syndrome

Trisomy 13

Complete Trisomy 13 Syndrome

Trisomy 13 Syndrome

D1 Trisomy

Patau'S Syndrome

Complete Trisomy 13

Chromosome 13, Trisomy 13 Complete

D Trisomy Syndrome

Bartholin-Patau Syndrome

Chromosome 13 Duplication

D1 Trisomy Syndrome

D>1< Trisomy Syndrome

Patau

Chromosome 13 Trisomy

Abnormal Autosomes 13
Double Outlet Right Ventricle

Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect

Taussig-Bing Syndrome

Dextrotransposition Of Aorta

Taussig-Bing Syndrome Or Defect

Dorv

Dorv With Subpulmonary Vsd

Dorv-Tga

Double Outlet Right Ventricle With Transposition Of The Great Arteries

Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type

Taussig-Bing Heart

Taussig-Bing Malformation

Taussig-Bing Complex

Taussig-Bing Defect

Taussig-Bing

Double Outlet Right Ventricle With Remote Ventricular Septal Defect

Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect

Double Outlet Right Ventricle With Non-Committed Interventricular Communication

Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis

Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis
Hereditary Angioedema

Hereditary Angioneurotic Edema

Hereditary Angioedema Type 1

Hane

Angioedema, Hereditary

Hae

Angioedemas, Hereditary

Deficiency Of C1 Esterase Inhibitor

C1 Esterase Inhibitor Deficiency

C1 Inhibitor Deficiency

Familial Angioneurotic Edema

Hereditary Bradykinine-Induced Angioedema

Hereditary Non Histamine-Induced Angioedema

Hae 1

Hae-I

Hereditary Angioneurotic Edema Type 1

Hereditary C1 Esterase Inhibitor Deficiency - Deficient Factor

Hereditary Angioedema Types I And Ii

Hereditary Angioneurotic Oedema

Familial Angioedema

Hae - [Hereditary Angioneurotic Oedema]

Bannister Disease, Hereditary

Quincke Disease Or Oedema

Hereditary Quincke Oedema
Ventricular Septal Defect

Ventricular Septal Defects

Interventricular Septal Defect

Heart Septal Defects, Ventricular

Ventricular Septal Abnormality

Interventricular Septum Defect

Ventricular Septum Defect

Vsd - [Ventricular Septum Defect]

Congenital Ventricular Septal Defect

Single Ventricular Septal Defect
Patent Ductus Arteriosus 1

Patent Ductus Arteriosus

PDA1

Pda

Ductus Arteriosus, Patent

Patent Ductus Arteriosus, Susceptibility To

Patent Ductus Botalli

Patency Of The Ductus Arteriosus

Patent Ductus Arteriosus Familial

Ductus Arteriosus Patent

Patent Ductus Arteriosus - Persisting Type
Visceral Heterotaxy

Situs Ambiguus

Heterotaxia

Heterotaxy Syndrome

Heterotaxy

Lateralization Defect

Situs Ambiguous

Left Isomerism

Htx

Ivemark Syndrome

Right Isomerism

Situs Ambiguus Viscerum

Incomplete Situs Inversus

Partial Situs Inversus

Heterotaxy, Visceral

Asplenia Syndrome

Bilateral Left-Sidedness

Polysplenia Syndrome

Moller Syndrome
Tetralogy Of Fallot

TOF

Fallot Tetralogy

Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

Tetrad Of Fallot

Fallot Tetrad

Fallot Disease

Fallot Complex

Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

Interventricular Septal Defect, In Tetralogy Of Fallot

Ventricular Septal Defect With Obstructed Right Ventricular Outflow

Tof - [Tetralogy Of Fallot]

Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

Pulmonary Atresia, Ventricular Septal Defect And Mapcas

Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
Congenital Nervous System Abnormality

Congenital Neurologic Anomaly

Congenital Nervous System Disorder
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS05052 FOXH1 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus FOXH1 MGD MGI:1347465
Rattus norvegicus FOXH1 RGD RGD:1311275
Felis catus FOXH1 VGNC VGNC:62334
Canis familiaris FOXH1 VGNC VGNC:51772
Bos taurus FOXH1 VGNC VGNC:29086
Macaca mulatta FOXH1 VGNC VGNC:72699